2p15–p16.1 microdeletion syndrome: molecular characterization and association of the OTX1 and XPO1 genes with autism spectrum disorders

A noise-reduction GWAS analysis implicates altered regulation of neurite outgrowth and guidance in autism

(2011) John P Hussman et al.   Molecular Autism

Further characterization of microdeletion syndrome involving 2p15-p16.1

(2010) Têmis Maria Félix et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Variants in several genomic regions associated with asperger disorder

(2010) D. Salyakina et al.   Autism Research

Outcome of array CGH analysis for 255 subjects with intellectual disability and search for candidate genes using bioinformatics

(2010) Y. Qiao et al.   HUMAN GENETICS

A genome-wide scan for common alleles affecting risk for autism

(2010) R. Anney et al.   HUMAN MOLECULAR GENETICS

Expression of the Homeobox Genes OTX2 and OTX1 in the Early Developing Human Brain

(2010) Karen B. Larsen et al.   JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY

A Genome-wide Association Study of Autism Reveals a Common Novel Risk Locus at 5p14.1

(2009) Deqiong Ma et al.   ANNALS OF HUMAN GENETICS

A Genome-Wide Association Study of Social and Non-Social Autistic-Like Traits in the General Population Using Pooled DNA, 500 K SNP Microarrays and Both Community and Diagnosed Autism Replication Samples

(2009) Angelica Ronald et al.   BEHAVIOR GENETICS

Autism-associated familial microdeletion of Xp11.22

(2009) Y Qiao et al.   CLINICAL GENETICS

A newly recognised microdeletion syndrome of 2p15-16.1 manifesting moderate developmental delay, autistic behaviour, short stature, microcephaly, and dysmorphic features: a new patient with 3.2 Mb deletion

(2009) J-S Liang et al.   JOURNAL OF MEDICAL GENETICS

A genome-wide linkage and association scan reveals novel loci for autism

(2009) Lauren A. Weiss et al.   NATURE

Duplications of noncoding elements 5′ of SOX9 are associated with brachydactyly-anonychia

(2009) Ingo Kurth et al.   NATURE GENETICS

Structural Variation of Chromosomes in Autism Spectrum Disorder

(2008) Christian R. Marshall et al.   AMERICAN JOURNAL OF HUMAN GENETICS

A Common Genetic Variant in the Neurexin Superfamily Member CNTNAP2 Increases Familial Risk of Autism

(2008) Dan E. Arking et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Novel Submicroscopic Chromosomal Abnormalities Detected in Autism Spectrum Disorder

(2008) Susan L. Christian et al.   BIOLOGICAL PSYCHIATRY

The DLX1and DLX2 genes and susceptibility to autism spectrum disorders

(2008) Xudong Liu et al.   EUROPEAN JOURNAL OF HUMAN GENETICS